Mondays and Tuesdays: 08:00-12:00 and by appointment

Registration:
Mondays to Thursdays:
08:00-15:30
Fridays: 08:00-14:00

Treatment and care of children and adolescents with a congenital disorder of the immune system (also suspected).

Our range of services:

• Immunodeficiencies in children and adolescents
• Severe combined immunodeficiencies (SCID)
• Combined immunodeficiencies (incl. DNA repair defects such as ataxia teleangiectasia)
• Syndromic immunodeficiencies (e.g. immunoosseous dysplasia, DiGeorge syndrome (22q11))
• Antibody deficiency diseases (e.g. hypogammaglobulinemia, CVID, agammaglobulinemia or Bruton's disease)
• Diseases with immune dysregulation (e.g. APDS, APECED, IPEX, STAT3, STAT1, CTLA-4, HLH syndromes such as XIAP)
• Phagocyte defects (e.g. septic granulomatosis, leukocyte adhesion defects (LAD))
• Disorders of the congenital immune system (e.g. IRAK4, MyD88, MSMD (lack of defense against mycobacteria))
• Autoinflammation (interferonopathies and periodic fever syndromes such as PFAPA, CAPS, TRAPS, ADA2)
• Complement defects (Bruton's bus), diseases with immune dysregulation (e.g. APDS, APECED, IPEX, STAT3, STAT1, CTLA-4, HLH syndromes such as XIAP)
• Phagocyte defects (e.g. septic granulomatosis, leukocyte adhesion defects (LAD))
  

Mondays: 08:00-11:30/ 13:30-15:00
Tuesdays: 08:00-12:00/14:00-15:15
Wednesdays: 08:00-12:00 a.m.
Fridays: 08:00-09:00 (joint puncture aftercare)

Interdisciplinary consultation (with the Annastift pediatric orthopaedics department):
Tuesdays: 08:00-12:30 (every 1st Tuesday/ every 2 months)

Transition consultation (transition consultation for adolescents aged 16 and over together with Dr. K. Rosenthal, internal rheumatologist, Hanover):
Wednesdays: 13:30-15:00 (every 1st Wednesday of the month)

Joint consultation with the pediatric dermatologist PD Dr. Hagen Ott: 1 x per quarter

Treatment of all forms of rheumatic diseases in children and adolescents (rheumatism).

Our range of services:

• Oligoarthritis
• seronegative and seropositive polyarthritis
• Systemic form (Still's disease)
• Enthesitis-associated JIA
• Psoriatic arthritis
• collagenoses
• Systemic lupus erythematosus
• Juvenile dermatomyositis

All forms of scleroderma:

• Morphea
• Linear form
• Systemic form
• Vasculitides (Kawasaki syndrome, Schönlein-Henoch purpura, PAN and others)
• Periodic fever syndromes (familial Mediterranean fever, TRAPS and others)
• Chronic non-bacterial osteitis (CNO)
• Pain intensification syndromes